Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

2017 ◽  
Vol 19 (6) ◽  
pp. 1454-1461 ◽  
Author(s):  
Maurice A. Marsini ◽  
Frederic G. Buono ◽  
Jon C. Lorenz ◽  
Bing-Shiou Yang ◽  
Jonathan T. Reeves ◽  
...  

A convergent and robust synthesis of a developmental CCR1 antagonist is described using continuous flow technology.

Author(s):  
Jessica Orrego‐Hernández ◽  
Helen Hölzel ◽  
Maria Quant ◽  
Zhihang Wang ◽  
Kasper Moth‐Poulsen

Author(s):  
Jessica Orrego-Hernández ◽  
Helen Hölzel ◽  
Maria Quant ◽  
Zhihang Wang ◽  
Kasper Moth-Poulsen

Synthesis ◽  
2012 ◽  
Vol 44 (15) ◽  
pp. 2469-2473 ◽  
Author(s):  
Jing Liu ◽  
Anne Fitzgerald ◽  
Neelakandha Mani

Nanoscale ◽  
2020 ◽  
Vol 12 (23) ◽  
pp. 12647-12654
Author(s):  
Yingyan Zhou ◽  
Dumei Wang ◽  
Xueming Kang ◽  
Dongtang Zhang ◽  
Xiangnan Dou ◽  
...  

An array-channel continuous flow scale-up strategy based on a microchip for high dispersion of loaded PtFeCu/C nanocatalysts for nanomaterials’ synthesis is reported.


2019 ◽  
Vol 9 (24) ◽  
pp. 6841-6851 ◽  
Author(s):  
Romaric Gérardy ◽  
Julien Estager ◽  
Patricia Luis ◽  
Damien P. Debecker ◽  
Jean-Christophe M. Monbaliu

A scalable intensified flow process for the preparation of cyclic organic carbonates relying on a cheap ammonium organocatalyst.


2020 ◽  
Vol 74 (11) ◽  
pp. 890-894
Author(s):  
Eimear Hegarty ◽  
Francesca Paradisi

Significant progress has been made in establishing transaminases as robust biocatalysts for the green and scalable synthesis of a diverse range of chiral amines. However, very few examples on the amination of small cyclic ketones have been reported. Cyclic ketones are particularly challenging for transaminase enzymes because they do not display the well-defined small and large substituent areas that are characteristic for the bio- catalytic mechanism. In this work, we exploited the broad substrate scope of the (S)-selective transaminase from Halomonas elongata (HeWT) to develop an efficient biocatalytic system in continuous flow to generate a range of small cyclic amines which feature very often in pharmaceuticals and agrochemicals. [3] Tetrahydrofuran-3-one and other challenging prochiral ketones were rapidly (5–45 min) transformed to their corresponding amines with excellent molar conversion (94–99%) and moderate to excellent ee.


2012 ◽  
Vol 1 (1) ◽  
pp. 24-27 ◽  
Author(s):  
Alicia C. Gutierrez ◽  
Timothy F. Jamison

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